Which of the follow reactions would produce a ketone?

Q: Name the product of the esterificaticn reaction of the two compounds shown here OH Но O ethyl…

A: The reaction is as follows:

Q: (1) Cl,, NAOH (2) H,O*

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Q: What role does an alkyl group have in the following reactions: SN1 SN2 E1 E2

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Q: elimination substitution addition rearrangement

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Q: **ーく CHCH,OH 。 ちと。みぶ

A: in the following case , 1-2 - addition pdt is the major pdt, because electrophilicityof the…

Q: Which of the following will deprotonate an aldehyde to a large degree (almost completely)? A) sodium…

A: Deprotonation of aldehyde is done by base. Hence, strongest base will deprotonate completely.  E.…

Q: This question is about the reaction scheme shown CH₂ CH₂ step 2 step 1 NO₂ NH₂ Amine A CH₂ step 3…

A: Amines are the organic compounds that can be primary, secondary or tertiary.

Q: Rank the following compounds from most reactive to least reactive in an electrophilic aromatic…

A: Electrophilic aromatic substitution: In an organic reaction in which an electrophile replaced an…

Q: How would you synthesize allyl ketones and diketones starting from acetoacetic ester?

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Q: What is the name of each compound that is formed in each of the reaction?

A: The details solution for this reaction is provided below in attach image.

Q: What is the major product to the following elimination reaction? NaOH 'CI

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Q: Provide reagents/conditions to accomplish the following syntheses. Several steps are required in…

A: In this question, we will provide reagents/conditions ( conditions like using solvent or heating )…

Q: List the appropriate reagents that can be used in places with questions in the following series of…

A: Organic reactions involve organic molecules. We can use specific reagents to obtain the desired…

Q: Draw the major organic product(s) of the following reaction. Br NaSCH 3 acetonitrile

A: Here we have to write the major product of given reaction-

Q: Predict the direction of equilibrium in the following reaction. Explain your answer. O NH₂ + NH3

A: Ka and PKa tells the relative acidity of compounds

Q: what is the reaction for getting a carboxylic acid from C10H13BrO?

A: C10H13BrO is chemical compound having Carbon, Hydrogen, Oxygen, Bromine with molecular weight 229.11…

Q: Ketones and aldehydes react with sodium acetylide (the sodium salt of acetylene) to give alcohols,…

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Q: What is the major product to the following elimination reaction? CI DBU

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Q: Complete the elimination reactions shown below. a. Br Br Br Br KOH A KOtBu butanol propanol

A: KOH acts as strong base where KOtBu acts as base as well as nucleophile, But KOtBu works at less…

Q: Rank the following carboxylic acid derivatives in decreasing order (most to least) of reactivity…

A: Acid chloride is the most reactive followed by  ester and amide is the  stable. Carboxylate ion is…

Q: Draw the products of the following reaction, then upload all drawings to the question at the end.

A: Organic reactions are reactions in which organic reactants react with each other to give organic…

Q: Predict the major product of the following reaction and draw it in the space provided. 1) NH,NH, 2)…

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Q: halides would you start with to as the major 3) What alkg! of the following get each

A: Elimination reaction of alkyl halide: Alkyl halide gives an elimination reaction by reacting with a…

Q: Which of the following are not related as a keto-enol pair? он and HO and Он and and ÓH

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Q: Predict the major product of the following reaction. NaOH ÅH 'H H₂O

A: Carbonyl compounds containing at least one alpha hydrogen on treatment with base undergo aldol…

Q: What reagent would you use to distinguish between a ketone and methylketone and indicate what you…

A: The structure of ketone: Where , R and R' can be same or different alkyl groups(other than methyl)…

Q: Tollowing IIkely HO HO LOH ОН

A: Interpretation: We have to tell which among the following will most easily form lactone.

Q: Predict the organic product of the reaction. Include all hydrogen atoms

A: In the presence of sulfuric acid, alkene undergoes to hydration to produce alcohol. The kinetic of…

Q: Provide the missing reactants and reagents. a is bis c is d is a e is C of ↑ NHCH3…

A: The synthesis of the compound involves  Friedelcraft reaction,oxidation, reduction

Q: Provide a detailed electron pushing mechanism describing the following conversion HCI Меон 'N. Br2…

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Q: 01: Find the weight of NA2C204 (FW= 134.00 g/mol) required to prepare 250 mL of 0.1000 M NazC204…

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Q: CH;CH, -NH, + CH, C-OH A product of the reaction above would be a(n) alkene salt O secondary amine O…

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Q: Which of the reaction conditions could afford the following transformation?

A: Here in this reaction we have to 1st abstract acidic proton of alkyne by an base like (NaNH2) and…

Q: Match the product in (Columns )when the following compounds in (Rows) are oxidized with K2Cr2O7?…

A: Esterification: It is the process of formation of ester by the reaction between an alcohol and an…

Q: The products in the following reaction are incorrect, briefly explain why the products are…

A: Given is organic reaction. The given products are incorrect. The given reaction is,

Q: Which of the following carbonyl compounds will react with phosphonium ylides to make alkenes? You…

A: Here we have to explain this using the mechanism of each and every reaction

Q: How would you explain the o-p directing formation of phenol, while nitro benzene is m directional?…

A: By drawing resonating strutures of phenol and nitrobenzene we can explain their directing behaviour.

Q: Rank the following compounds in order of increasing basicity. CH3 H3C CH3 H3C 00 KO 11 CH3 CH3 IV A)…

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Q: What is the major organic product from the following reaction? IV 11 OH NaOH/H₂O A OH OH III

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: The major product that will form during the nitration of benzoic acid is? OA H-N OR ON oc OD. COOH…

A:

Reactions of Ethers

Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and behavior of ethers are discussed in the context of organic chemistry.

Epoxides

Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic.

Williamson Ether Synthesis

An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction.